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FDA 510(k)

CUSTOM TRAYS, KITS

K-Number: K894610 · 1990-03-15

Decision Date1990-03-15
Product CodeFSM
Advisory CommitteeSU
DecisionUnknown

Device Summary

CUSTOM TRAYS, KITS is the device name listed in this FDA 510(k) record. The listed applicant is L H M Ent., Inc.. It received FDA 510(k) clearance on 1990-03-15 under 510(k) number K894610. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CUSTOM TRAYS, KITS?

CUSTOM TRAYS, KITS is a medical device that received FDA 510(k) clearance on 1990-03-15. The listed applicant is L H M Ent., Inc.. The 510(k) number is K894610.

When did CUSTOM TRAYS, KITS receive FDA 510(k) clearance?

CUSTOM TRAYS, KITS received FDA 510(k) clearance on 1990-03-15, under 510(k) number K894610.

Who is the listed applicant for CUSTOM TRAYS, KITS?

The FDA 510(k) record lists L H M Ent., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUSTOM TRAYS, KITS?

The FDA product code for CUSTOM TRAYS, KITS is FSM.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing L H M Ent., Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FSM)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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